Colon Cancer: Gene >> KCNK6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263372
Start	38326809:38326809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567646784
CDS Mutation	c.539T>C
AA Mutation	p.Val180Ala(p.V180A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263372
Start	38327399:38327399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938G>T
AA Mutation	p.Arg313Met(p.R313M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263372
Start	38327246:38327246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785T>C
AA Mutation	p.Leu262Pro(p.L262P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263372
Start	38326660:38326660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263372
Start	38326609:38326609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774603954
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263372
Start	38326807:38326807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368336056
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263372
Start	38327283:38327283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142781541
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK6

No Mutation Annotation!